Skanray Technologies Limited

Skanray Technologies Limited — FDA 510(k) Submissions

Skanray Technologies Limited has submitted 4 FDA 510(k) premarket notifications since 2022, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, X-ray, Stationary, System, X-ray, Mobile, Interventional Fluoroscopic X-ray System . Use the specialty filter in the sidebar to narrow results.